Genes underlying delayed puberty

This publication has 97 references indexed in Scilit:

• Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
  New England Journal of Medicine, 2013
• Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement
  Nature Genetics, 2012
• Leptin action in pubertal development: recent advances and unanswered questions
  Trends in Endocrinology & Metabolism, 2012
• Heparan sulfate 6-O-sulfotransferase 1 , a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism
  Proceedings of the National Academy of Sciences, 2011
• Loss-of-Function Mutations in RAB18 Cause Warburg Micro Syndrome
  The American Journal of Human Genetics, 2011
• Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
  Nature Genetics, 2010
• Gene networks and the neuroendocrine regulation of puberty
  Molecular and Cellular Endocrinology, 2010
• Meta-analysis of genome-wide association data identifies two loci influencing age at menarche
  Nature Genetics, 2009
• Genetic variation in LIN28B is associated with the timing of puberty
  Nature Genetics, 2009
• Menopause and the human hypothalamus: Evidence for the role of kisspeptin/neurokinin B neurons in the regulation of estrogen negative feedback
  Peptides, 2009